Label: PINK EYE RELIEF- belladonna, euphrasia officinalis, hepar sulphuris solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 53799-365-11 - Packager: Similasan AG
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated October 7, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Active ingredients
- Purpose
- Active ingredients
- Purpose
- Uses*
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Warnings
• For external use only.
• Children under 2 years of age should be seen by a physician.
• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).
• To avoid contamination, do not touch the tip of the bottle to any surface.
• To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle.
• Replace cap tightly after every use.
• ‡Our drops will not harm contact lenses, however we recommend not wearing contacts while experiencing eye irritation.
- Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PINK EYE RELIEF
belladonna, euphrasia officinalis, hepar sulphuris solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53799-365 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 6 [hp_X] in 10 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 10 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SILVER SULFATE (UNII: 8QG6HV4ZPO) SODIUM NITRATE (UNII: 8M4L3H2ZVZ) SODIUM BORATE (UNII: 91MBZ8H3QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53799-365-11 10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 02/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/01/2017 Labeler - Similasan AG (481545754)